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dc.contributor.authorMichelozzi, IM
dc.contributor.authorSufi, J
dc.contributor.authorAdejumo, TA
dc.contributor.authorAmrolia, PJ
dc.contributor.authorTape, CJ
dc.contributor.authorGiustacchini, A
dc.date.accessioned2022-05-27T09:27:03Z
dc.date.available2022-05-27T09:27:03Z
dc.identifier.citationSTAR protocols, 2022, 3 (1), pp. 101174 - ?en
dc.identifier.issn2666-1667
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5153
dc.identifier.eissn2666-1667en_US
dc.identifier.eissn2666-1667
dc.identifier.doi10.1016/j.xpro.2022.101174en_US
dc.identifier.doi10.1016/j.xpro.2022.101174
dc.description.abstractHere, we present a comprehensive protocol for the generation and functional characterization of chimeric antigen receptor (CAR) T cells and their products by mass cytometry in a reproducible and scalable manner. We describe the production of CAR T cells from human peripheral blood mononuclear cells. We then detail a three-step staining protocol with metal-labeled antibodies and the subsequent mass cytometry analysis. This protocol allows simultaneous characterization of CAR T cell intracellular signaling, activation, proliferation, cytokine production, and phenotype in a single assay.en_US
dc.formatElectronic-eCollectionen_US
dc.format.extent101174 - ?en_US
dc.languageengen_US
dc.language.isoengen
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectLeukocytes, Mononuclearen_US
dc.subjectT-Lymphocytesen_US
dc.subjectHumansen_US
dc.subjectAntibodiesen_US
dc.titleHigh-dimensional functional phenotyping of preclinical human CAR T cells using mass cytometry.en
dc.typeJournal Article
dcterms.dateAccepted2022-03-18
rioxxterms.versionVoRen
rioxxterms.versionofrecord10.1016/j.xpro.2022.101174en
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0en
dc.relation.isPartOfSTAR protocolsen_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Oncogene
pubs.publication-statusPublisheden_US
pubs.volume3en_US
pubs.embargo.termsNot knownen_US
icr.researchteamOncogene
dc.contributor.icrauthorTape, Christopher


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/